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FDA 510(k)

NAUTIFLUX

K-Number: K060010 · 2006-08-04

ApplicantSedat
Decision Date2006-08-04
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NAUTIFLUX is the device name listed in this FDA 510(k) record. The listed applicant is Sedat. It received FDA 510(k) clearance on 2006-08-04 under 510(k) number K060010. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAUTIFLUX?

NAUTIFLUX is a medical device that received FDA 510(k) clearance on 2006-08-04. The listed applicant is Sedat. The 510(k) number is K060010.

When did NAUTIFLUX receive FDA 510(k) clearance?

NAUTIFLUX received FDA 510(k) clearance on 2006-08-04, under 510(k) number K060010.

Who is the listed applicant for NAUTIFLUX?

The FDA 510(k) record lists Sedat as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NAUTIFLUX?

The FDA product code for NAUTIFLUX is DQO.

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Other records listing Sedat as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K082755SEDAT FLAMINGOK080472SEDAT MYSHELL LITE

Related Devices (Code: DQO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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